Found: 35
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Positional cloning identifies a novel cyclophilin as a candidate amplified oncogene in 1q21.
- Published in:
- Oncogene, 2002, v. 21, n. 14, p. 2261, doi. 10.1038/sj.onc.1205339
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- Publication type:
- Article
Frequent cases of RAS-mutated Down syndrome acute lymphoblastic leukaemia lack JAK2 mutations.
- Published in:
- Nature Communications, 2014, v. 5, n. 8, p. 4654, doi. 10.1038/ncomms5654
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- Publication type:
- Article
Ectopic sequences from truncated HMGIC in liposarcomas are derived from various amplified chromosomal regions.
- Published in:
- Genes, Chromosomes & Cancer, 2001, v. 31, n. 3, p. 264, doi. 10.1002/gcc.1143
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- Publication type:
- Article
Narrowing of the region of allelic loss in 21q11-21 in squamous non-small cell lung carcinoma and cloning of a novel ubiquitin-specific protease gene from the deleted segment.
- Published in:
- Genes, Chromosomes & Cancer, 2000, v. 27, n. 2, p. 153, doi. 10.1002/(SICI)1098-2264(200002)27:2<153::AID-GCC6>3.0.CO;2-A
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- Publication type:
- Article
Increased levels of a chromosome 21-encoded tumour invasion and metastasis factor (TIAM1) mRNA in bone marrow of down syndrome children during the acute phase of AML(M7).
- Published in:
- Genes, Chromosomes & Cancer, 1998, v. 23, n. 1, p. 61, doi. 10.1002/(SICI)1098-2264(199809)23:1<61::AID-GCC9>3.0.CO;2-4
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- Publication type:
- Article
Tumour angiogenesis is reduced in the Tc1 mouse model of Down’s syndrome.
- Published in:
- 2010
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- Publication type:
- Correction notice
Tumour angiogenesis is reduced in the Tc1 mouse model of Down’s syndrome.
- Published in:
- Nature, 2010, v. 465, n. 7299, p. 813, doi. 10.1038/nature09106
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- Publication type:
- Article
A genetic cause of Alzheimer disease: mechanistic insights from Down syndrome.
- Published in:
- 2015
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- Publication type:
- Journal Article
A genetic cause of Alzheimer disease: mechanistic insights from Down syndrome.
- Published in:
- Nature Reviews Neuroscience, 2015, v. 16, n. 9, p. 564, doi. 10.1038/nrn3983
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- Publication type:
- Article
Ultrastructural and dynamic studies of the endosomal compartment in Down syndrome.
- Published in:
- Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. 1, doi. 10.1186/s40478-020-00956-z
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- Publication type:
- Article
Mechanical Stress Induces a Transient Suppression of Cytokine Secretion in Astrocytes Assessed at the Single‐Cell Level with a High‐Throughput Microfluidic Chip.
- Published in:
- Advanced Healthcare Materials, 2021, v. 10, n. 21, p. 1, doi. 10.1002/adhm.202100698
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- Publication type:
- Article
Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex.
- Published in:
- Journal of Investigative Dermatology, 2005, v. 124, n. 5, p. 998, doi. 10.1111/j.0022-202X.2005.23675.x
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- Publication type:
- Article
Human Epidermal Differentiation Complex in a Single 2.5 Mbp Long Continuum of Overlapping DNA Cloned in Bacteria Integrating Physical and Transcript Maps.
- Published in:
- Journal of Investigative Dermatology, 1999, v. 112, n. 6, p. 910, doi. 10.1046/j.1523-1747.1999.00613.x
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- Publication type:
- Article
An additional human chromosome 21 causes suppression of neural fate of pluripotent mouse embryonic stem cells in a teratoma model.
- Published in:
- BMC Developmental Biology, 2007, v. 7, p. 131, doi. 10.1186/1471-213X-7-131
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- Publication type:
- Article
Amplified segment in the 'Down Syndrome critical region' on HSA21 shared between Down syndrome and euploid AML-M0 excludes RUNX1, ERG and ETS2.
- Published in:
- British Journal of Haematology, 2012, v. 157, n. 2, p. 197, doi. 10.1111/j.1365-2141.2011.08985.x
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- Publication type:
- Article
Genome gains at chromosome 21q21/22 segment leads to co-amplification of Down Syndrome Critical Regions and known oncogenes in a case of donor cell-derived acute myeloid leukaemia following allogeneic sex mismatched umbilical cord blood transplantation for chronic myeloid leukaemia
- Published in:
- 2010
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- Publication type:
- Letter
Loss-of-function JAK3 mutations in TMD and AMKL of Down syndrome.
- Published in:
- British Journal of Haematology, 2007, v. 137, n. 4, p. 337, doi. 10.1111/j.1365-2141.2007.06574.x
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- Publication type:
- Article
Microarray transcript profiling distinguishes the transient from the acute type of megakaryoblastic leukaemia (M7) in Down's syndrome, revealing PRAME as a specific discriminating marker.
- Published in:
- British Journal of Haematology, 2004, v. 125, n. 6, p. 729, doi. 10.1111/j.1365-2141.2004.04982.x
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- Publication type:
- Article
Alzheimer‐like pathology in trisomy 21 cerebral organoids amenable to pharmacological inhibition reveals BACE2 as a gene‐dose‐sensitive AD‐suppressor in human brain: Development of new models and analysis methods: Multisystem platform models of ADRD
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.043136
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- Publication type:
- Article
TRISOMY 21 CAUSES A DEFICIT IN LYSOSOMAL CATHEPSINS AND ALTERS APP/Aβ PROCESSING, INDEPENDENTLY OF AN EXTRA COPY OF APP.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P661, doi. 10.1016/j.jalz.2017.06.791
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- Publication type:
- Article
Health comorbidities and cognitive abilities across the lifespan in Down syndrome.
- Published in:
- Journal of Neurodevelopmental Disorders, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s11689-019-9306-9
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- Publication type:
- Article
Brief Report: Isogenic Induced Pluripotent Stem Cell Lines From an Adult With Mosaic Down Syndrome Model Accelerated Neuronal Ageing and Neurodegeneration.
- Published in:
- Stem Cells, 2015, v. 33, n. 6, p. 2077, doi. 10.1002/stem.1968
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- Publication type:
- Article
Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemia.
- Published in:
- Nature Genetics, 2001, v. 28, n. 3, p. 220, doi. 10.1038/90054
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- Publication type:
- Article
Inter-Dependent Mechanisms Behind Cognitive Dysfunction, Vascular Biology and Alzheimer’s Dementia in Down Syndrome: Multi-Faceted Roles of APP.
- Published in:
- Frontiers in Behavioral Neuroscience, 2015, v. 9, p. 1, doi. 10.3389/fnbeh.2015.00299
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- Publication type:
- Article
Differential Coassembly of α1-GABA<sub>A</sub>Rs Associated with Epileptic Encephalopathy.
- Published in:
- Journal of Neuroscience, 2020, v. 40, n. 29, p. 5518, doi. 10.1523/JNEUROSCI.2748-19.2020
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- Publication type:
- Article
Publisher Correction: Genetic dissection of down syndrome‑associated alterations in APP/amyloid‑β biology using mouse models.
- Published in:
- 2021
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- Publication type:
- Correction Notice
Genetic dissection of down syndrome-associated alterations in APP/amyloid-β biology using mouse models.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-85062-3
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- Publication type:
- Article
Validating the Cognitive Scale for Down Syndrome (CS-DS) to Detect Longitudinal Cognitive Decline in Adults With Down Syndrome.
- Published in:
- Frontiers in Psychiatry, 2019, p. N.PAG, doi. 10.3389/fpsyt.2019.00158
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- Publication type:
- Article
Neurofilament light as a blood biomarker for neurodegeneration in Down syndrome.
- Published in:
- Alzheimer's Research & Therapy, 2018, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13195-018-0367-x
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- Publication type:
- Article
Genes and Mechanisms Modulating Ageing and Neurodegeneration Derived From Studying Down Syndrome.
- Published in:
- 2020
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- Publication type:
- Abstract
Cytogenetic and molecular study of 32 Down syndrome families: potential leukaemia predisposing role of the most proximal segment of chromosome 21q.
- Published in:
- British Journal of Haematology, 1998, v. 103, n. 1, p. 213, doi. 10.1046/j.1365-2141.1998.00924.x
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- Publication type:
- Article
Association of Dementia With Mortality Among Adults With Down Syndrome Older Than 35 Years.
- Published in:
- JAMA Neurology, 2019, v. 72, n. 6, p. 152, doi. 10.1001/jamaneurol.2018.3616
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- Publication type:
- Article
Model for a transcript map of human chromosome 21: isolation of new coding sequences from exon and enriched cDNA libraries.
- Published in:
- Human Molecular Genetics, 1995, v. 4, n. 8, p. 1291
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- Publication type:
- Article
An integrated YAC-overlap and ‘cosmid-pocket’ map of the human chromosome 21.
- Published in:
- Human Molecular Genetics, 1994, v. 3, n. 5, p. 759
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- Publication type:
- Article
DNA-Methylation Patterns in Trisomy 21 Using Cells from Monozygotic Twins.
- Published in:
- PLoS ONE, 2015, v. 10, n. 8, p. 1, doi. 10.1371/journal.pone.0135555
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- Publication type:
- Article